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186 results on '"Pauri, Flavia"'

3. Infectious risk in multiple sclerosis patients treated with disease-modifying therapies: A three-year observational cohort study

Author

Zingaropoli, Maria Antonella, primary, Pasculli, Patrizia, additional, Iannetta, Marco, additional, Perri, Valentina, additional, Tartaglia, Matteo, additional, Crisafulli, Sebastiano Giuseppe, additional, Merluzzo, Chiara, additional, Baione, Viola, additional, Mazzochi, Lorenzo, additional, Taglietti, Ambra, additional, Pauri, Flavia, additional, Frontoni, Marco, additional, Altieri, Marta, additional, Gaeta, Aurelia, additional, Antonelli, Guido, additional, Conte, Antonella, additional, Mastroianni, Claudio Maria, additional, and Ciardi, Maria Rosa, additional

Published
2022
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4. Assessment and management of infectious risk in multiple sclerosis patients treated with disease-modifying therapies

Author

Zingaropoli, Maria Antonella, Pasculli, Patrizia, Iannetta, Marco, Perri, Valentina, Tartaglia, Matteo, Crisafulli, Sebastiano Giuseppe, Merluzzo, Chiara, Baione, Viola, Mazzocchi, Lorenzo, Taglietti, Ambra, Pauri, Flavia, Frontoni, Marco, Altieri, Marta, Gaeta, Aurelia, Antonelli, Guido, Conte, Antonella, Mastroianni, Claudio, and Ciardi, Maria Rosa

Published
2021
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6. Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity

Author

Stevanin, Giovanni, Montagna, Giorgia, Azzedine, Hamid, Valente, Enza Maria, Durr, Alexandra, Scarano, Valentina, Bouslam, Naima, Cassandrini, Denise, Denora, Paola S., Criscuolo, Chiara, Belarbi, Soraya, Orlacchio, Antonio, Jonveaux, Philippe, Silvestri, Gabriella, Hernandez, Anne Marie Ouvrad, De Michele, Giuseppe, Tazir, Meriem, Mariotti, Caterina, Brockmann, Knut, Malandrini, Alessandro, van der Knapp, Marjo S., Neri, Marcella, Tonekaboni, Hassan, Melone, Mariarosa A. B., Tessa, Alessandra, Dotti, M. Teresa, Tosetti, Michela, Pauri, Flavia, Federico, Antonio, Casali, Carlo, Cruz, Vitor T., Loureiro, José L., Zara, Federico, Forlani, Sylvie, Bertini, Enrico, Coutinho, Paula, Filla, Alessandro, Brice, Alexis, and Santorelli, Filippo M.

Published
2006
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9. Screening of ARHSP-TCC Patients Expands the Spectrum of SPG11 Mutations and Includes a Large Scale Gene Deletion

Author

Denora, Paola S., Schlesinger, David, Casali, Carlo, Kok, Fernando, Tessa, Alessandra, Boukhris, Amir, Azzedine, Hamid, Teresa Dotti, Maria, Bruno, Claudio, Truchetto, Jeremy, Biancheri, Roberta, Fedirko, Estelle, Di Rocco, Maja, Bueno, Clarissa, Malandrini, Alessandro, Battini, Roberta, Sickl, Elisabeth, de Leva, Maria Fulvia, Boespflug-Tanguy, Odile, Silvestri, Gabriella, Simonati, Alessandro, Said, Edith, Ferbert, Andreas, Criscuolo, Chiara, Heinimann, Karl, Modoni, Anna, Weber, Peter, Palmeri, Silvia, Plasilova, Martina, Pauri, Flavia, Cassandrini, Denise, Battisti, Carla, Pini, Antonella, Tosetti, Michela, Hauser, Erwin, Masciullo, Marcella, Di Fabio, Roberto, Piccolo, Francesca, Denis, Elodie, Cioni, Giovanni, Massa, Roberto, Giustina, Elvio Della, Calabrese, Olga, Melone, Marina A.B., De Michele, Giuseppe, Federico, Antonio, Bertini, Enrico, Durr, Alexandra, Brockmann, Knut, Knaap, Marjo S. van der, Zatz, Mayana, Filla, Alessandro, Brice, Alexis, Stevanin, Giovanni, and Santorelli, Filippo M.

Published
2009
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17. Withdrawal from acute medication normalises short-term cortical synaptic potentiation in medication overuse headache

Author

Cortese, Francesca, primary, Pierelli, Francesco, additional, Pauri, Flavia, additional, Di Lorenzo, Cherubino, additional, Lepre, Chiara, additional, Malavolta, Giulia, additional, Merluzzo, Chiara, additional, Parisi, Vincenzo, additional, Ambrosini, Anna, additional, Serrao, Mariano, additional, and Coppola, Gianluca, additional

Published
2019
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20. Coexistence of contralateral cluster headache and probable paroxysmal hemicrania: a case report

Author

Pauri Flavia and Lepre Chiara

Subjects
Multidisciplinary, Case Study, business.industry, Cluster headache, cluster headache, chemical and pharmacologic phenomena, medicine.disease, stomatognathic diseases, 03 medical and health sciences, 0302 clinical medicine, stomatognathic system, Unilateral Headaches, 030220 oncology & carcinogenesis, Anesthesia, medicine, Paroxysmal Hemicrania, hypothalamus, paroxysmal hemicrania, multidisciplinary, business, 030217 neurology & neurosurgery
Abstract

Introduction The trigeminal autonomic cephalagias (TACs) are short-lasting unilateral headaches associated with autonomic features. Even if coexistence of different ipsilateral TACs in the same patient has been previously reported in few papers, the simultaneous occurrence of contralateral TACs is not described previously. Case description A 50 years old working man complained, at the end of his cluster period, a new TAC, fitting the criteria for probable paroxysmal hemicrania. The dramatic improvement of this last cephalalgia with indomethacin treatment confirmed the diagnosis. Discussion, evaluation and conclusion There is a clear overlap in clinical diagnosis between cluster headache (CH) and paroxysmal hemicrania (PH) and similarities are somewhat greater than differences. The originality of this report is the coexistence of contralateral TACs in the same patients at the same moment. According neuroimaging studies, CH hypothalamic activation occurs ipsilateral to the side of the headache while in PH hypothalamic activation occurs contralateral to the side of headache. It could be suggested that a continuous hypothalamic activation give a maladaptive plasticity recruiting closed neuronal aggregates responsible for the developing of PH after a long period of CH, confirming the central origin of both CH and PH. Further studies need to confirm this hypothesis.

Published
2016

22. Evidence for rapid brain morphometric changes during the migraine cycle

Author

Coppola, G, Di Renzo, A, Tinelli, Emanuele, Iacovelli, E, Lepre, C, Dilorenzo, C, Dilorenzo, G, Dilenola, D, Parisi, V, Serrao, Mariano, Pauri, Flavia, Fiermonte, Giancarlo, Bianco, Federico, and Pierelli, Francesco

Subjects
brain morphometric changes, Headache, mri
Published
2014

46. Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity

Author

Giovanni, Stevanin, Giorgia, Montagna, Hamid, Azzedine, Enza Maria Valente, Alexandra, Durr, Valentina, Scarano, Naima, Bouslam, Denise, Cassandrini, Denora, Paola S., Chiara, Criscuolo, Soraya, Belarbi, Antonio, Orlacchio, Philippe, Jonveaux, Gabriella, Silvestri, Anne Marie Ouvrad Hernandez, De Michele, G., Meriem, Tazir, Caterina, Mariotti, Knut, Brockmann, Alessandro, Malandrini, Van Der Knapp, M. S., Marcella, Neri, Hassan, Tonekaboni, Melone, Mariarosa A. B., Alessandra, Tessa, Teresa Dotti, M., Michela, Tosetti, Pauri, Flavia, Antonio, Federico, Casali, Carlo, Cruz, Vitor T., Loureiro, Jose L., Federico, Zara, Sylvie, Forlani, Enrico, Bertini, Paula, Coutinho, Alessandro, Filla, Alexis, Brice, Santorelli, Filippo M., Casali, C., Neurologie et thérapeutique expérimentale, Université Pierre et Marie Curie - Paris 6 (UPMC)-IFR70-Institut National de la Santé et de la Recherche Médicale (INSERM), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Unit of Molecular Medicine, IRCCS, Mendel Institute, Department of Neurological Sciences, University of Naples Federico II = Università degli studi di Napoli Federico II, Pediatric Neurology and Neuromuscular Diseases Unit, Università degli studi di Genova = University of Genoa (UniGe), Service de Neurologie, Hopital Mustapha, Department of Neurosciences, Università degli Studi di Roma Tor Vergata [Roma], Service de Génétique [CHRU Nancy], Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy), Department of Neuroscience, Catholic University, Département de neurologie, Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble, Besta Neurological Institute, Department of Pediatrics and Neuropediatrics, Georg-August-University = Georg-August-Universität Göttingen, Institute of Neurological Sciences, Department of Child Neurology, VU University Medical Center [Amsterdam], Medical Genetics, Università degli Studi di Ferrara = University of Ferrara (UniFE), Stella Maris, Department of Neurology and ORL, Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome] (UNIROMA), Departamento de Neurologia, Hospital S. Sebastiao, ANR-05-MRAR-0001,Cav3pathies,Approches physiopathologique et moléculaire de la signalisation calcique dans les caveolinopathies musculaires(2005), Stevanin, G, Montagna, G, Azzedine, H, Valente, Em, Durr, A, Scarano, V, Bouslam, N, Cassandrini, D, Denora, P, Criscuolo, C, Belarbi, S, Orlacchio, A, Jonveaux, P, Silvestri, G, Hernandez, Am, DE MICHELE, G, Tazir, M, Mariotti, C, Brockmann, K, Malandrini, A, VAN DER KNAPP, M, Neri, M, Tonekaboni, H, Melone, Mariarosa Anna Beatrice, Tessa, A, Dotti, Mt, Tosetti, M, Pauri, F, Federico, A, Casali, C, Cruz, Vt, Loureiro, Jl, Zara, F, Forlani, S, Bertini, E, Coutinho, P, Filla, A, Brice, A, Santorelli, Fm, Pediatric surgery, Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR70-Université Pierre et Marie Curie - Paris 6 (UPMC), Service de Génétique Cytogénétique et Embryologie [CHU Pitié-Salpêtrière], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Università degli studi di Napoli Federico II, Universita degli studi di Genova, Georg-August-University [Göttingen], Università degli Studi di Ferrara (UniFE), University of Naples Federico II, and Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome]

Subjects
Male, Candidate gene, Genetic Linkage, Corpus Callosum, Consanguinity, Autosomal recessive hereditary spastic, Genetic heterogeneity, 0302 clinical medicine, MESH: Child, Spastic Paraplegia, Autosomal recessive hereditary spastic paraplegia, Linkage, SPG11, Thin corpus callosum, Adolescent, Child, Child, Preschool, Chromosomes, Human, Pair 15, Female, Humans, Infant, Lod Score, Pedigree, Phenotype, Spastic Paraplegia, Hereditary, Genes, Recessive, Genetic Heterogeneity, Genetics, Genetics (clinical), Cellular and Molecular Neuroscience, 0303 health sciences, MESH: Spastic Paraplegia, Hereditary, MESH: Genetic Heterogeneity, MESH: Infant, autosomal recessive hereditary spastic paraplegia, genetic heterogeneity, linkage, spg11, thin corpus callosum, Hereditary, Settore MED/26 - Neurologia, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Human, Hereditary spastic paraplegia, MESH: Pedigree, Locus (genetics), Biology, MESH: Phenotype, MESH: Corpus Callosum, Chromosomes, 03 medical and health sciences, Gene mapping, Genetic linkage, medicine, Recessive, Preschool, MESH: Genes, Recessive, 030304 developmental biology, MESH: Adolescent, MESH: Consanguinity, Autosome, MESH: Humans, Thin corpus callosum, SPG11, Linkage, Haplotype, MESH: Child, Preschool, Pair 15, medicine.disease, MESH: Male, Genes, MESH: Lod Score, MESH: Linkage (Genetics), MESH: Female, 030217 neurology & neurosurgery, MESH: Chromosomes, Human, Pair 15
Abstract

We studied 20 Mediterranean families (40 patients) with autosomal recessive hereditary spastic paraplegia and thin corpus callosum (ARHSP-TCC, MIM 604360) to characterize their clinical and genetic features. In six families (17 patients) of Algerian Italian, Moroccan, and Portuguese ancestry, we found data consistent with linkage to the SPG11 locus on chromosome 15q13-15, whereas, in four families (nine patients of Italian, French, and Portuguese ancestry) linkage to the SPG11 locus could firmly be excluded, reinforcing the notion that ARHSP-TCC is genetically heterogeneous. Patients from linked and unlinked families could not be distinguished on the basis of clinical features alone. In SPG11-linked kindred, haplotype reconstruction allowed significant refinement to 6 cM, of the minimal chromosomal interval, but analysis of two genes (MAP1A and SEMA6D) in this region did not identify causative mutations. Our findings suggest that ARHSP-TCC is the most frequent form of ARHSP in Mediterranean countries and that it is particularly frequent in Italy.

Published
2006

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